基于谷胱甘肽响应的多白藜芦醇纳米颗粒有效的药物传递和逆转多药耐药。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Yang Liping, He Jian, Tao Zhenchao, Zhou Yan, Yang Jing, Zhang Yangyang, Gao Jing, Qian Liting
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引用次数: 11

摘要

癌症对人类健康构成严重威胁,是导致人类死亡的最常见原因。聚合物基纳米药物目前被用于提高化疗药物的治疗效果和降低全身毒性。然而,目前聚合物载体的缺点是没有治疗程序。本文首次以白藜芦醇(RES)和3,3′-二硫代二丙酸为原料,采用缩聚-聚合的方法合成了具有抗癌作用的谷胱甘肽(GSH)响应聚合物(PRES)。PRES不仅可以抑制肿瘤细胞的生长,还可以自组装成纳米颗粒(~ 93 nm),用于输送抗肿瘤药物,如紫杉醇(PTX@PRES NPs)。该系统可实现高载药量(~ 7%)并克服多药耐药(MDR)。体外实验结果表明,PRES形成的NPs在体循环中稳定,在肿瘤细胞高GSH环境中可有效降解。细胞毒性实验结果证实PTX@PRES NPs能有效抑制癌细胞(A549)和耐药细胞(A549/PTX)的生长。NPs还可以显著提高药物对A549/PTX荷瘤小鼠的治疗效果。体内研究也表明,基于press的NPs具有肿瘤抑制作用。综上所述,我们合成的gsh响应聚合物具有多种有趣的功能,可以用于有效的药物传递。该聚合物具有良好的治疗效果,可用于耐多药的治疗。因此,该合成系统可用于开发治疗癌症的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

GSH-responsive poly-resveratrol based nanoparticles for effective drug delivery and reversing multidrug resistance.

GSH-responsive poly-resveratrol based nanoparticles for effective drug delivery and reversing multidrug resistance.

GSH-responsive poly-resveratrol based nanoparticles for effective drug delivery and reversing multidrug resistance.

GSH-responsive poly-resveratrol based nanoparticles for effective drug delivery and reversing multidrug resistance.

Cancer poses a serious threat to human health and is the most common cause of human death. Polymer-based nanomedicines are presently used to enhance the treatment effectiveness and decrease the systemic toxicity of chemotherapeutic agents. However, the disadvantage of currently polymeric carriers is without therapy procedure. Herein, for the first time, glutathione (GSH)-responsive polymer (PRES) with anti-cancer effect was synthesized following the condensation-polymerization method using resveratrol (RES) and 3,3'-dithiodipropionic acid. PRES can not only suppress the tumor cells growth but can also self-assemble into nanoparticles (∼93 nm) for delivering antitumor drugs, such as paclitaxel (PTX@PRES NPs). The system could achieve high drug loading (∼7%) and overcome multidrug resistance (MDR). The results from the in vitro studies revealed that the NPs formed of PRES were stable in the systemic circulation, while could be efficiently degraded in tumor cells high GSH environment. Results from cytotoxicity tests confirmed that PTX@PRES NPs could effectively suppress the growth of cancer cells (A549) and drug-resistant cells (A549/PTX). The NPs could also be used to significantly increase the therapeutic efficacy of the drugs in A549/PTX tumor-bearing mice. In vivo investigations also demonstrated that the PRES-based NPs exhibited tumor inhibition effects. In summary, we report that the GSH-responsive polymer synthesized by us exhibited multiple interesting functions and could be used for effective drug delivery. The polymer exhibited good therapeutic effects and could be used to overcome MDR. Thus, the synthesized system can be used to develop a new strategy for treating cancer.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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